Literature DB >> 336093

Structural heterogeneity of the cytoplasmic and outer membranes of Escherichia coli.

L De Leij, B Witholt.   

Abstract

The cytoplasmic and outer membranes of gram-negative bacteria can be isolated from spheroplasts, and separated on sucrose density gradients. Lysis of spheroplasts causes extensive membrane fragmentation and since the characteristics of the fragments obtained by different lysis procedures need not be identical, the influence of the disruption method on membrane composition has been examined. Spheroplasts of Escherichia coli J5 were lysed by osmotic shock, which did not significantly separate the cytoplasmic and outer membranes, but resulted in mixed membrane vesicles. Lysis in the French press and by sonication caused extensive membrane fragmentation and separation. Sonication, however, also caused some fusion between fragments of the outer and the cytoplasmic membranes; this intermembrane fusion increased with sonication time. When the cytoplasmic and outer membranes were well separated and intermembrane fusion was minimal or absent, the cytoplasmic and outer membrane fragments were heterogeneous with respect to density and ovarll phospholipid, protein and lipopolysaccharide composition. In addition, cytoplasmic, but not outer, membrane fragments were also heterogeneous with respect to protein composition. It is concluded, therefore, that membrane fragments obtained from the cytoplasmic and outer membranes are heterogeneous independently of the lysis procedures used to obtain these fragments. Possible reasons for this heterogeneity are discussed.

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Year:  1977        PMID: 336093     DOI: 10.1016/0005-2736(77)90396-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Biological characterization of an Enterobacter cloacae outer membrane protein (OmpX).

Authors:  J Stoorvogel; M J van Bussel; J A van de Klundert
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

Review 2.  Lipid trafficking across the Gram-negative cell envelope.

Authors:  Rahul Shrivastava; Shu-Sin Chng
Journal:  J Biol Chem       Date:  2019-08-16       Impact factor: 5.157

3.  Unequal distribution of penicillin-binding proteins among inner membrane vesicles of Escherichia coli.

Authors:  G H Jacoby; K D Young
Journal:  J Bacteriol       Date:  1988-08       Impact factor: 3.490

4.  Preparation of the FhuA (TonA) receptor protein from cell envelopes of an overproducing strain of Escherichia coli K-12.

Authors:  H Hoffmann; E Fischer; H Kraut; V Braun
Journal:  J Bacteriol       Date:  1986-05       Impact factor: 3.490

5.  Biosynthesis and turnover of outer-membrane proteins in Escherichia coli ML308-225.

Authors:  R J Allen; G K Scott
Journal:  Biochem J       Date:  1979-08-15       Impact factor: 3.857

6.  Enzymology, genetics, and regulation of membrane phospholipid synthesis in Escherichia coli.

Authors:  C R Raetz
Journal:  Microbiol Rev       Date:  1978-09

7.  K88-mediated binding of Escherichia coli outer membrane fragments to porcine intestinal epithelial cell brush borders.

Authors:  J M Middeldorp; B Witholt
Journal:  Infect Immun       Date:  1981-01       Impact factor: 3.441

8.  Separation of Escherichia coli penicillin-binding proteins into different membrane vesicles by agarose electrophoresis and sizing chromatography.

Authors:  M J Leidenix; G H Jacoby; T A Henderson; K D Young
Journal:  J Bacteriol       Date:  1989-10       Impact factor: 3.490

9.  Identification and localization of two membrane-bound esterases from Escherichia coli.

Authors:  M Pacaud
Journal:  J Bacteriol       Date:  1982-01       Impact factor: 3.490

10.  Biophysical studies of the membrane-embedded and cytoplasmic forms of the glucose-specific Enzyme II of the E. coli phosphotransferase system (PTS).

Authors:  Mohammad Aboulwafa; Milton H Saier
Journal:  PLoS One       Date:  2011-09-15       Impact factor: 3.240

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